(Q32145046)

English

autosomal recessive osteopetrosis 2

osteopetrosis characterized by autosomal recessive inheritance that has material basis in homozygous mutation in the TNFSF11 gene on chromosome 13q14

  • OPTB2
  • mild autosomal recessive form osteopetrosis
  • osteoclast-poor osteopetrosis
  • Osteopetrosis autosomal recessive 2
  • Osteopetrosis osteoclast-poor
  • Osteopetrosis, Autosomal Recessive type 2
  • OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2; OPTB2
  • Osteopetrosis, Osteoclast-Poor
  • OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2
  • Osteopetrosis, Mild Autosomal Recessive Form
  • autosomal recessive osteopetrosis type 2
In more languages
default values for all languages
No label defined

No description defined

Statements

Identifiers

 
edit
    edit
      edit
        edit
          edit
            edit
              edit
                edit
                  edit